Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.

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New trends in aminoglycosides use.An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.

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Q33951177-B1C132B1-E3AB-4B3C-B434-4BFD7796676A Q34955098-59FB7EF6-1039-41D3-9221-CF68DEFA3362

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Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Maternally transmitted aminogl ...... gene in two Chinese families.

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Cheng Liu

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Dan Xu

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Guangqian Xing

http://www.w3.org/2001/XMLSchema#string

Haifeng Li

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Qinjun Wei

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Xin Cao

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Xingkuan Bu

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Yajie Lu

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Zhibin Chen

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P2860

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China

Sequence and gene organization of mouse mitochondrial DNA

Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

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98-103

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scholarly article

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10.3109/14992027.2012.743046

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2012-12-13T00:00:00Z

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23237192

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Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.

about

P2860

P2860

Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.

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P698